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Normobaric Oxygen Therapy for Individuals With First-Episode Psychosis

Primary Purpose

Psychosis, Schizophrenia, First-episode Psychosis

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Normobaric Oxygen
Placebo
Sponsored by
Nicholas Breitborde
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Psychosis focused on measuring psychosis, treatment, normobaric hyperoxia

Eligibility Criteria

15 Years - 35 Years (Child, Adult)All SexesDoes not accept healthy volunteers
  • Diagnosis of a schizophrenia-spectrum disorder or mood disorder with psychotic features as determined using the Structured Clinical Interview for the DSM-5.
  • Less than 5 years since the onset of frank psychotic symptoms as determined using the Symptom Onset in Schizophrenia Inventory .
  • No evidence of a pre-existing intellectual disability defined as a premorbid IQ >70 as estimated using the Reading subtest of the Wide Range Achievement Test-4.
  • Ages 15-35
  • Non-smoker for past six months
  • Absence of suicidal ideation or behavior over the past month as assessed by the Columbia Suicide Severity Rating Scale
  • The American Association for Respiratory Care notes that "no absolute contraindications to oxygen therapy exist when indications [for oxygen therapy] are present."

Sites / Locations

  • Harding HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Normobaric Oxygen Therapy (40% FiO2)

Placebo Condition

Arm Description

4 weeks of nightly normobaric oxygen therapy (40% FiO2)

4 weeks of a placebo condition utilizing room air oxygen levels (21% FiO2)

Outcomes

Primary Outcome Measures

Change from baseline in cognitive functioning
Change in scores on the MATRICS Consensus Cognitive Battery (MCCB).
Change from baseline in quality of life
Change in scores on WHO Quality of Life Scale Brief (WHOQOL-BREF.
Change from baseline in social functioning
Change in scores on the Global Functioning: Social Scale. Scores on this measure range from 1-10 with higher scores indicating greater social functioning
Change from baseline in role functioning
Change in scores on the Global Functioning: Role Scale. Scores on this measure range from 1-10 with higher scores indicative of greater role functioning.
Change from baseline in health-related quality of life
Change in scores on the RAND 36-Item Health Survey.

Secondary Outcome Measures

Change from baseline in suicidality
Change in occurrence in suicidal thoughts or behaviors as assessed using the Columbia Suicide Severity Rating Scale. This is a categorical rating scale that identifies the presence or absence of specific levels of severity of suicidal ideation and behavior.
Change from baseline in substance use severity
Change in scores on the HABITS scale. This scale assesses the absolute values of use of specific substances (e.g., number of cigarettes smoked)
Change from baseline in service utilization
Change in scores on the Modified Service Use and Resources Form for Schizophrenia
Change in Sleep
Change in scores on the Pittsburgh Sleep Quality Index.
Change from baseline in medication adherence
Change in scores on the Medication Adherence rating Scale. Scores on this scale range from 0-10 with higher scores indicative of greater medication adherence.

Full Information

First Posted
April 27, 2020
Last Updated
July 31, 2023
Sponsor
Nicholas Breitborde
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1. Study Identification

Unique Protocol Identification Number
NCT04368039
Brief Title
Normobaric Oxygen Therapy for Individuals With First-Episode Psychosis
Official Title
Normobaric Oxygen Therapy for Individuals With First-Episode Psychosis
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
December 4, 2019 (Actual)
Primary Completion Date
December 7, 2025 (Anticipated)
Study Completion Date
December 7, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Nicholas Breitborde

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
No

5. Study Description

Brief Summary
Single-blind, randomized controlled trial of normobaric oxygen therapy among individuals with first-episode psychosis: Effects on symptomatology and cognition.
Detailed Description
Functional deficits in prefrontal, limbic, and temporal regions of the brain are well-documented among individuals with psychotic disorders. Mitochondrial dysfunction may contribute to such pathology, and effective functioning of mitochondrial activity in the brain in dependent on a sufficient supply of oxygen. These data suggest that oxygen therapy may improve symptoms in individuals with psychosis. This small pilot study will test this hypothesis. Individuals with first-episode psychosis will be randomized to receive either (i) 4 weeks of nightly normobaric oxygen therapy (40% FiO2) or (ii) 4 weeks of a placebo condition utilizing room air oxygen levels (21% FiO2). Participants will be blinded to what condition they receive. Both conditions will be delivered via nasal cannula connected to oxygen concentrators at five liters per minute (lpm), and participants will be instructed to complete the intervention overnight while sleeping. At the end of the 4 week period, all individuals will receive an additional 4 weeks of unblinded (i.e., "open label") nightly normobaric oxygen therapy (40% FiO2). Study assessments will be completed at (i) enrollment; (ii) 4 weeks after enrollment, and (iii) 8 weeks after enrollment.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psychosis, Schizophrenia, First-episode Psychosis
Keywords
psychosis, treatment, normobaric hyperoxia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Normobaric Oxygen Therapy (40% FiO2)
Arm Type
Experimental
Arm Description
4 weeks of nightly normobaric oxygen therapy (40% FiO2)
Arm Title
Placebo Condition
Arm Type
Placebo Comparator
Arm Description
4 weeks of a placebo condition utilizing room air oxygen levels (21% FiO2)
Intervention Type
Device
Intervention Name(s)
Normobaric Oxygen
Intervention Description
40% FiO2 for 4 weeks
Intervention Type
Device
Intervention Name(s)
Placebo
Intervention Description
21% FiO2 for 4 weeks
Primary Outcome Measure Information:
Title
Change from baseline in cognitive functioning
Description
Change in scores on the MATRICS Consensus Cognitive Battery (MCCB).
Time Frame
4 weeks
Title
Change from baseline in quality of life
Description
Change in scores on WHO Quality of Life Scale Brief (WHOQOL-BREF.
Time Frame
4 weeks
Title
Change from baseline in social functioning
Description
Change in scores on the Global Functioning: Social Scale. Scores on this measure range from 1-10 with higher scores indicating greater social functioning
Time Frame
4 weeks
Title
Change from baseline in role functioning
Description
Change in scores on the Global Functioning: Role Scale. Scores on this measure range from 1-10 with higher scores indicative of greater role functioning.
Time Frame
4 weeks
Title
Change from baseline in health-related quality of life
Description
Change in scores on the RAND 36-Item Health Survey.
Time Frame
4 weeks
Secondary Outcome Measure Information:
Title
Change from baseline in suicidality
Description
Change in occurrence in suicidal thoughts or behaviors as assessed using the Columbia Suicide Severity Rating Scale. This is a categorical rating scale that identifies the presence or absence of specific levels of severity of suicidal ideation and behavior.
Time Frame
4 weeks
Title
Change from baseline in substance use severity
Description
Change in scores on the HABITS scale. This scale assesses the absolute values of use of specific substances (e.g., number of cigarettes smoked)
Time Frame
4 weeks
Title
Change from baseline in service utilization
Description
Change in scores on the Modified Service Use and Resources Form for Schizophrenia
Time Frame
4 weeks
Title
Change in Sleep
Description
Change in scores on the Pittsburgh Sleep Quality Index.
Time Frame
4 weeks
Title
Change from baseline in medication adherence
Description
Change in scores on the Medication Adherence rating Scale. Scores on this scale range from 0-10 with higher scores indicative of greater medication adherence.
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Diagnosis of a schizophrenia-spectrum disorder or mood disorder with psychotic features as determined using the Structured Clinical Interview for the DSM-5. Less than 5 years since the onset of frank psychotic symptoms as determined using the Symptom Onset in Schizophrenia Inventory . No evidence of a pre-existing intellectual disability defined as a premorbid IQ >70 as estimated using the Reading subtest of the Wide Range Achievement Test-4. Ages 15-35 Non-smoker for past six months Absence of suicidal ideation or behavior over the past month as assessed by the Columbia Suicide Severity Rating Scale The American Association for Respiratory Care notes that "no absolute contraindications to oxygen therapy exist when indications [for oxygen therapy] are present."
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Nicholas Breitborde, PhD
Phone
(614) 685-6052
Email
nicholas.breitborde@osumc.edu
Facility Information:
Facility Name
Harding Hospital
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Nicholas Breitborde, PhD
Phone
614-685-6052
Email
nicholas.breitborde@osumc.edu

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
15352925
Citation
Hill K, Mann L, Laws KR, Stephenson CM, Nimmo-Smith I, McKenna PJ. Hypofrontality in schizophrenia: a meta-analysis of functional imaging studies. Acta Psychiatr Scand. 2004 Oct;110(4):243-56. doi: 10.1111/j.1600-0447.2004.00376.x.
Results Reference
background
PubMed Identifier
15038995
Citation
Karry R, Klein E, Ben Shachar D. Mitochondrial complex I subunits expression is altered in schizophrenia: a postmortem study. Biol Psychiatry. 2004 Apr 1;55(7):676-84. doi: 10.1016/j.biopsych.2003.12.012.
Results Reference
background
PubMed Identifier
17092996
Citation
Kann O, Kovacs R. Mitochondria and neuronal activity. Am J Physiol Cell Physiol. 2007 Feb;292(2):C641-57. doi: 10.1152/ajpcell.00222.2006. Epub 2006 Nov 8.
Results Reference
background
PubMed Identifier
22722511
Citation
Bloch Y, Applebaum J, Osher Y, Amar S, Azab AN, Agam G, Belmaker RH, Bersudsky Y. Normobaric hyperoxia treatment of schizophrenia. J Clin Psychopharmacol. 2012 Aug;32(4):525-30. doi: 10.1097/JCP.0b013e31825d70b8.
Results Reference
background
Citation
First, M.B., et al., Structured Clinical Interview for DSM-5-Research Version2015, Arlington, VA: American Psychiatric Association.
Results Reference
background
PubMed Identifier
10867307
Citation
Perkins DO, Leserman J, Jarskog LF, Graham K, Kazmer J, Lieberman JA. Characterizing and dating the onset of symptoms in psychotic illness: the Symptom Onset in Schizophrenia (SOS) inventory. Schizophr Res. 2000 Jul 7;44(1):1-10. doi: 10.1016/s0920-9964(99)00161-9.
Results Reference
background
Citation
Wilkinson, G.S. and G.J. Robertson, Wide Range Achievement Test (WRAT4)2006, Lutz, FL: PAR, Inc.
Results Reference
background
PubMed Identifier
22193671
Citation
Posner K, Brown GK, Stanley B, Brent DA, Yershova KV, Oquendo MA, Currier GW, Melvin GA, Greenhill L, Shen S, Mann JJ. The Columbia-Suicide Severity Rating Scale: initial validity and internal consistency findings from three multisite studies with adolescents and adults. Am J Psychiatry. 2011 Dec;168(12):1266-77. doi: 10.1176/appi.ajp.2011.10111704.
Results Reference
background
PubMed Identifier
17715561
Citation
AARC. AARC clinical practice guideline. Oxygen therapy in the home or alternate site health care facility--2007 revision & update. Respir Care. 2007 Aug;52(8):1063-8. No abstract available.
Results Reference
background
Citation
Schizophrenia Spectrum and Other Psychotic Disorders, in DSM-5® Clinical Cases.
Results Reference
background
Citation
Auther, A., C. Smith, and B. Cornblatt, Global Functioning: Social Scale (GF: Social). Glen Oaks, NY: Zucker-Hillside Hospital, 2006.
Results Reference
background
Citation
Niendam, T., et al., Global Functioning: Role Scale (GF: Role). Los Angeles, CA: University of California, Los Angeles, 2006.
Results Reference
background
PubMed Identifier
17151158
Citation
Rosenheck RA, Leslie DL, Sindelar J, Miller EA, Lin H, Stroup TS, McEvoy J, Davis SM, Keefe RS, Swartz M, Perkins DO, Hsiao JK, Lieberman J; CATIE Study Investigators. Cost-effectiveness of second-generation antipsychotics and perphenazine in a randomized trial of treatment for chronic schizophrenia. Am J Psychiatry. 2006 Dec;163(12):2080-9. doi: 10.1176/ajp.2006.163.12.2080.
Results Reference
background
PubMed Identifier
18172019
Citation
Nuechterlein KH, Green MF, Kern RS, Baade LE, Barch DM, Cohen JD, Essock S, Fenton WS, Frese FJ 3rd, Gold JM, Goldberg T, Heaton RK, Keefe RS, Kraemer H, Mesholam-Gately R, Seidman LJ, Stover E, Weinberger DR, Young AS, Zalcman S, Marder SR. The MATRICS Consensus Cognitive Battery, part 1: test selection, reliability, and validity. Am J Psychiatry. 2008 Feb;165(2):203-13. doi: 10.1176/appi.ajp.2007.07010042. Epub 2008 Jan 2.
Results Reference
background
PubMed Identifier
9626712
Citation
Development of the World Health Organization WHOQOL-BREF quality of life assessment. The WHOQOL Group. Psychol Med. 1998 May;28(3):551-8. doi: 10.1017/s0033291798006667.
Results Reference
background
PubMed Identifier
10785582
Citation
Thompson K, Kulkarni J, Sergejew AA. Reliability and validity of a new Medication Adherence Rating Scale (MARS) for the psychoses. Schizophr Res. 2000 May 5;42(3):241-7. doi: 10.1016/s0920-9964(99)00130-9.
Results Reference
background
Citation
Hays, R.D., S. Prince-Embury, and H.Y. Chen, RAND-36 Health Status Inventory1998, San Antonio, TX: The Psychological Corporation.
Results Reference
background
PubMed Identifier
3774930
Citation
Levine J, Schooler NR. SAFTEE: a technique for the systematic assessment of side effects in clinical trials. Psychopharmacol Bull. 1986;22(2):343-81. No abstract available.
Results Reference
background
PubMed Identifier
2748771
Citation
Buysse DJ, Reynolds CF 3rd, Monk TH, Berman SR, Kupfer DJ. The Pittsburgh Sleep Quality Index: a new instrument for psychiatric practice and research. Psychiatry Res. 1989 May;28(2):193-213. doi: 10.1016/0165-1781(89)90047-4.
Results Reference
background
PubMed Identifier
15753237
Citation
Palmer BA, Pankratz VS, Bostwick JM. The lifetime risk of suicide in schizophrenia: a reexamination. Arch Gen Psychiatry. 2005 Mar;62(3):247-53. doi: 10.1001/archpsyc.62.3.247.
Results Reference
background

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Normobaric Oxygen Therapy for Individuals With First-Episode Psychosis

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